Clinical Results of High-Dose Chemotherapy Followed by Autologous Peripheral Blood Stem Cell Transplantation in Children with Advanced Stage Rhabdomyosarcoma

被引:7
作者
Kim, Nam Kyun [1 ]
Kim, Hyo Sun [1 ]
Suh, Chang-Ok [2 ]
Kim, Hyun Ok [3 ]
Lyu, Chuhl Joo [1 ]
机构
[1] Yonsei Univ Hlth Syst, Dept Pediat, Seoul, South Korea
[2] Yonsei Univ Hlth Syst, Dept Radiat Oncol, Seoul, South Korea
[3] Yonsei Univ Hlth Syst, Dept Lab Med, Seoul, South Korea
关键词
Rhabdomyosarcoma; Children; Chemotherapy; Bone Marrow Transplantation; INTERGROUP RHABDOMYOSARCOMA; METASTATIC RHABDOMYOSARCOMA; UNDIFFERENTIATED SARCOMA; RISK RHABDOMYOSARCOMA; IV; ADOLESCENTS; IFOSFAMIDE; EXPERIENCE; ETOPOSIDE; THERAPY;
D O I
10.3346/jkms.2012.27.9.1066
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Regardless of improvement in cure of Rhabdomyosarcoma (RMS), the results in treatment of advanced stage of RMS in children are still dismal. Recently, high-dose chemotherapy followed by autologous peripheral blood stem cell transplantation (HDC/APBSCT) has been tried to manage the advanced high-risk RMS patients. We investigated the effectiveness of HDC/APBSCT by reviewing the clinical records of high-risk pediatric RMS patients in single institute database. Over twenty years, 37 patients were diagnosed as RMS with high-risk at the time of first diagnosis. These patients were classified as two groups according to treatment method. The first group was HDC/APBSCT and the other was conventional multi-agent chemotherapy group. Differences of clinical results between the two groups were analyzed. The median age of patients was 5 yr, ranging from 6 months to 15 yr. The 5-yr event free survival rate (EFS) of all patients was 24.8% +/- 4.8%. HDC/APBSCT group and conventional multi-agent chemotherapy group were 41.3% +/- 17.8% and 16.7% +/- 7.6% for 5-yr EFS, respectively (P = 0.023). There was a significant difference in the result of HDC/APBSCT between complete remission or very good partial response group and poor response group (50% +/- 20.4% vs 37.5% +/- 28.6%, P = 0.018). HDC/APBSCT can be a promising treatment modality in high-risk RMS patients.
引用
收藏
页码:1066 / 1072
页数:7
相关论文
共 23 条
[1]   A feasibility, toxicity, and early response study of etoposide, ifosfamide, and vincristine for the treatment of children with rhabdomyosarcoma: A report from the intergroup rhabdomyosarcoma study (IRS) IV pilot study [J].
Arndt, C ;
Tefft, M ;
Gehan, E ;
Anderson, J ;
Jenson, M ;
Link, M ;
Donaldson, S ;
Breneman, J ;
Wiener, E ;
Webber, B ;
Maurer, H .
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 1997, 19 (02) :124-129
[2]   Treatment of intermediate risk rhabdomyosarcoma and undifferentiated sarcoma with alternating cycles of vincristine/doxorubicin/cyclophosphamide and etoposide/ifosfamide [J].
Arndt, CAS ;
Nascimento, AG ;
Schroeder, G ;
Schomberg, PJ ;
Neglia, JP ;
Sencer, SF ;
Silberman, TL ;
Moertel, CL ;
Tillisch, JK ;
Miser, JS .
EUROPEAN JOURNAL OF CANCER, 1998, 34 (08) :1224-1229
[3]   High-dose chemotherapy in soft tissue sarcoma in children [J].
Atra, A ;
Pinkerton, R .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2002, 41 (02) :191-196
[4]   Benefit of intensified therapy for patients with local or regional embryonal rhabdomyosarcoma: Results from the Intergroup Rhabdomyosarcoma Study IV [J].
Baker, KS ;
Anderson, JR ;
Link, MP ;
Grier, HE ;
Qualman, SJ ;
Maurer, HM ;
Breneman, JC ;
Wiener, ES ;
Crist, WM .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (12) :2427-2434
[5]   Rhabdomyosarcoma: New windows of opportunity [J].
Breitfeld, PP ;
Meyer, WH .
ONCOLOGIST, 2005, 10 (07) :518-527
[6]   Prognostic factors and clinical outcomes in children and adolescents with metastatic rhabdomyosarcoma - A report from the intergroup rhabdomyosarcoma study IV [J].
Breneman, JC ;
Lyden, E ;
Pappo, AS ;
Link, MP ;
Anderson, JR ;
Parham, DM ;
Qualman, SJ ;
Wharam, MD ;
Donaldson, SS ;
Maurer, HM ;
Meyer, WH ;
Baker, KS ;
Paidas, CN ;
Crist, WM .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (01) :78-84
[7]   THE THIRD INTERGROUP RHABDOMYOSARCOMA STUDY [J].
CRIST, W ;
GEHAN, EA ;
RAGAB, AH ;
DICKMAN, PS ;
DONALDSON, SS ;
FRYER, C ;
HAMMOND, D ;
HAYS, DM ;
HERRMANN, J ;
HEYN, R ;
JONES, PM ;
LAWRENCE, W ;
NEWTON, W ;
ORTEGA, J ;
RANEY, RB ;
RUYMANN, FB ;
TEFFT, M ;
WEBBER, B ;
WIENER, E ;
WHARAM, M ;
VIETTI, TJ ;
MAURER, HM .
JOURNAL OF CLINICAL ONCOLOGY, 1995, 13 (03) :610-630
[8]   Poor outcome of two children with relapsed state stage IV alveolar rhabdomyosarcoma after allogeneic stem cell transplantation [J].
Doelken, R ;
Weigel, S ;
Schueler, F ;
Doelken, G ;
Beck, JF .
PEDIATRIC HEMATOLOGY AND ONCOLOGY, 2005, 22 (08) :699-703
[9]   The role of high-dose therapy and autologous stem cell transplantation for pediatric bone and soft tissue sarcomas [J].
Ek, Eugene T. H. ;
Choong, Peter F. M. .
EXPERT REVIEW OF ANTICANCER THERAPY, 2006, 6 (02) :225-237
[10]  
García-Alonso I, 2005, REV ESP ENFERM DIG, V97, P240